Shenzhen Changkun Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Pelvic Floor Rehabilitation Therapy Device (PD2301/PD2302/PD2303), Electric Breast Pump, Finger Pulse Oximeter, Model: X1906P
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Shenzhen Changkun Technology Co., Ltd. Gastroenterology & Urology ✕
1 devices